TRIETHYL 2-PHOSPHONOPROPIONATE
TRIETHYL 2-PHOSPHONOPROPIONATE Basic information
- Product Name:
- TRIETHYL 2-PHOSPHONOPROPIONATE
- Synonyms:
-
- TRIETHYL 2-PHOSPHONOPROPIONATE
- 2-DIETHYLPHOSPHONOPROPIONIC ACID ETHYL ESTER
- DIETHYL ETHOXYCARBONYLETHYL-PHOSPHONATE
- ETHYL-2-(DIETHYLPHOSPHONO)PROPANOATE
- Diethyl 1-(ethoxycarbonyl)ethanephosphonate~2-Phosphonopropionic acid triethyl ester
- Triethyl2-phosphonopropionate,98%
- 2-phosphonopropionic acid triethyl ester
- diethyl 1-(ethoxycarbonyl)ethanephosphonate
- CAS:
- 3699-66-9
- MF:
- C9H19O5P
- MW:
- 238.22
- EINECS:
- 223-033-4
- Product Categories:
-
- LJ
- Small molecule
- C-C Bond Formation
- Horner-Wadsworth-Emmons Reagents
- Olefination
- Mol File:
- 3699-66-9.mol
TRIETHYL 2-PHOSPHONOPROPIONATE Chemical Properties
- Melting point:
- 161-164°
- Boiling point:
- 143-144 °C12 mm Hg(lit.)
- Density
- 1.111 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.431(lit.)
- Flash point:
- 192 °F
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- Miscible with chloroform and methanol.
- form
- Liquid
- color
- Clear colorless
- Specific Gravity
- 1.111
- BRN
- 1786994
- InChIKey
- BVSRWCMAJISCTD-UHFFFAOYSA-N
- CAS DataBase Reference
- 3699-66-9(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38-38-37-36
- Safety Statements
- 23-24/25-36-26-39-37
- RIDADR
- 1993
- WGK Germany
- 3
- F
- 10
- Hazard Note
- Irritant
- HS Code
- 29319019
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
TRIETHYL 2-PHOSPHONOPROPIONATE Usage And Synthesis
Chemical Properties
CLEAR COLOURLESS LIQUID
Uses
Triethyl 2-Phosphonopropionate is used in studies involving insecticides and their efficacy on various bacterium. Also act as inhibitors of Epstein-Bar virus transmission and infections.
Uses
Triethyl 2-phosphonopropionate is used as a reactant in intramolecular conjugate addition for the synthesis of floresolide B, enantioselective synthesis of spiroindane di-methyl acetic acid and in stereo selective intramolecular Diels-Alder reactions. It plays an important role in Horner-Wadsworth-Emmons reactions and chemoenzymatic one-pot synthesis of gamma-butyrolactones. It is also used in the preparation of 3-[2]furyl-2-methyl-acrylic acid ethyl ester by reacting with furfural.
Purification Methods
Purify it by fractional distillation with high reflux ratio, preferably using a spinning band column. [Kosolapoff & Powell J Am Chem Soc 72 4198 1950, Kresze et al. Justus Liebigs Ann Chem 756 112 1972, Beilstein 4 IV 3617.]
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